MODIFIED SERIES 2100 ENDOSCOPES— 510(k) K912089
Substantially EquivalentMedical Laser, Inc.
FDA 510(k) clearance K912089 for MODIFIED SERIES 2100 ENDOSCOPES, Substantially Equivalent on 1991-08-12. Applicant: Medical Laser, Inc.. Device class: 2.
Clearance details
- Applicant
- Medical Laser, Inc.
- Product code
- Code ODF
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Minneapolis, MN, US
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